Recent advances in radical-mediated [2+2+m] annulation of 1,n-enynes
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摘要:
1,n-Enynes are a versatile class of unsaturated hydrocarbons that found broad applications in the synthetic community of natural products,biologically active structures and functional materials.Typical methods for the transformations of 1,n-enynes include the radical-mediated [2+2+m] annulation reaction as they are particularly efficient accesses to functionalized polycyclic compounds.We herein highlighted recent process in the radical-mediated [2+2+m] annulation of 1,n-enynes,including [2+2+1] and [2+2+2] modes,for the construction of five-to six-membered-ring-fused polycyclic scaffolds.Meanwhile,the mechanisms for these transformations were described.